|
Status |
Public on Apr 05, 2012 |
Title |
Hela input chromatin |
Sample type |
SRA |
|
|
Source name |
HeLa, input
|
Organism |
Homo sapiens |
Characteristics |
cell line: HeLa shRNA: none chip antibody: none growth protocol: Cells were grown in DMEM 10% FCS.
|
Treatment protocol |
HEK293 cells were stably infected with lentiviruses expressing the respective shRNAs or uninfected parent control.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
IPs from 2 ug of cross-linked extract were immunoprecipitated and prepared for Illumina library construction by repair with Klenow, T4 DNA polymerase and T4 polynucleotide kinase, A-tailing with Klenow exo-, ligation to branched adaptors, gel purification of ~200bp fragments, and amplification (18 cycles) with Illumina PE primers using Phusion DNA polymerase.
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina Genome Analyzer IIx |
|
|
Description |
Sheared input chromatin.
|
Data processing |
Single-end 34 base reads (after removing barcodes) were mapped to the hg18 UCSC human genome (Mar. 2006) with Bowtie version 0.12.5. Genome Build: hg18_input_hela__FC61ALD_6.wig.gz: hg18
|
|
|
Submission date |
Mar 08, 2012 |
Last update date |
May 15, 2019 |
Contact name |
David L. Bentley |
E-mail(s) |
david.bentley@ucdenver.edu
|
Organization name |
U. Colorado School of Medicine
|
Department |
Biochemistry and Mol. Genetics
|
Street address |
12801 E. 17th Ave
|
City |
Aurora |
State/province |
CO |
ZIP/Postal code |
80045 |
Country |
USA |
|
|
Platform ID |
GPL10999 |
Series (1) |
GSE36185 |
mRNA decapping factors and the exonuclease Xrn2 function in widespread premature termination of RNA polymerase II transcription |
|
Relations |
SRA |
SRX128190 |
BioSample |
SAMN00809669 |